Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 1
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 2
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 1
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 1
rs137852813
SOS1
0.807 0.200 2 39051202 missense variant A/C;G snv 1
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 1
rs397517153
SOS1
0.925 0.160 2 39022779 missense variant A/C;G snv 4.0E-06 1
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 2
rs397516830
RAF1
0.827 0.160 3 12604182 missense variant A/C;G;T snv 1
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 1
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 1
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 1
rs267607080
SOS1
0.925 0.160 2 39023134 missense variant A/G snv 1
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 1
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 1
rs397507523
PTPN11
0.882 0.160 12 112472954 missense variant A/G snv 1
rs397507529
PTPN11
0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 1
rs397507547
PTPN11
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06 1
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs397509345
PTPN11
0.851 0.160 12 112489093 missense variant AG/CC mnv 1
rs397517180
SOS1
0.925 0.160 2 39035440 missense variant C/A snv 1
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 2
rs180177036
BRAF
0.925 0.200 7 140778053 missense variant C/A;G snv 1
rs267607079
SOS1
0.776 0.240 2 39022772 missense variant C/A;G snv 1
rs397507506
PTPN11
0.807 0.240 12 112450354 missense variant C/A;G snv 1